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Lowongan Kerja Serang Posisi Qa Executive di Flexicare (Group) Limited

Gambar Flexicare (Group) Limited Posisi QA Executive

Loker diposting 2 tahun yang lalu

Perusahaan kami merilis lapangan pekerjaan dengan sistem full time untuk posisi QA Executive di kantor Flexicare (Group) Limited untuk daerah Serang serta sekitarnya.

Skill yang perusaahan inginkan ialah Manufaktur & Penjaminan Kualitas / QA serta orang yang mampu bekerja dengan tekun.

Selain itu untuk persyaratan yang kita butuhkan ialah min D3 (Diploma) & D4 (Diploma). Yang merupakan ketentuan yang usaha kami berikan.

Upah yang kami tawarkan cukup kompetitif menurut dari kemampuan karyawan. Rata-rata upah yang kami tawarkan adalah Rp 1.800.000 - Rp 5.500.000.

Info Loker

Perusahaan	Flexicare (Group) Limited
Posisi	Qa Executive
Tempat	Serang
Tingkatan Kerja	Supervisor/Koordinator
Kualifikasi	D3 (Diploma), D4 (Diploma)
Jenis Pekerjaan	Full Time
Spesialisasi Dibutuhkan	Manufaktur, Penjaminan Kualitas / QA
Gaji Min	Rp. 1.800.000
Gaji Max	Rp. 5.500.000

Description:

Quality Assurance Supervisor will establish quality regulations for products and employees. Should be able to analyse data in order to develop plans to motivate, and encourage employees while striving to improve processes and product quality.

He/ She should be able to plan and conduct validation activities, analyse data, and obtain relevant approvals. He/she should illustrate the required technical competencies in selecting proper methods, acceptance criteria, statistical techniques, sample size relevant to Injection moulding, Extrusion processes, ETO sterilization and sterile barrier system based on Flexicare group guidelines and ISO 13485 requirements.

Work location: Cikande

Responsibilities:

Product testing and defective product analysis;
Analysis of process defects and root cause of complaints, follow-up of complaints / preventive corrective actions;
Production of product inspection documents and related ISO forms;
New product verification;
New product testing and engineering improvement suggestions;
Preparation of quality inspection standard documents (QAS, Control Plan);
Handling and follow-up of customer complaints;
QA personnel training;
Operation monitoring of the quality management system;
Compilation and improvement of quality management system documents;
Auxiliary work for TUV Nord and CFDA audits;
Complete other tasks assigned by the leader.
Develop and Maintain validation plans and protocols that include methods, acceptance criteria, statistical techniques, sample size relevant to Injection molding and Extrusion processes
Proceed relevant verification and validations and obtain approvals prior introduction of new equipment, test methods, molds, measuring and monitoring units to the manufacturing processes.
Facilitate for the validation activities for sterilization and sterile barrier systems.
Proper record keeping and prompt report generation.
Technical support for plant trouble shooting activities along with maintenance department and ensure the conformity for the standard requirements.
Document Control for ISO 13485
Prepare SOP, WI, forms
Coordinate and work closely with ISO consultant to achieve ISO 13485 certificate

Qualifications

Engineering graduate from recognized University with Minimum 01-year experience in GMP environment.
Familiar with CAD programs like AutoCAD and SolidWorks
Experience in Validation in pharmaceutical / medical device industry will be added advantage.
Confidence
Excellent technical skills
Good numerical skills and an understanding of statistics
Leadership skills
Planning and organization skills
Communication and interpersonal skills
Problem-solving skills
Teamworking skills
IT skills
Ability to work independently
Confidence
Excellent technical skills
Good numerical skills and an understanding of statistics
Leadership skills
Planning and organization skills
Communication and interpersonal skills
Problem-solving skills
Teamworking skills
IT skills

Alamat Lengkap

Provinsi	Banten
Kota	Serang
Map	Google Map

Keuntungan Kerja

Yearly Bonus

Lamar kerja

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Lamar Sekarang Laporkan

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Deskripsi Perusahaan

Flexicare is a leading UK manufacturer of medical devices. Backed by over 30 years’ experience in design and development and supported by a modern manufacturing facility, Flexicare has built a world class reputation for the supply of medical devices. We currently supply anesthesia, respiratory care, critical care and urology products to more than 100 countries worldwide.The company has experienced sustained and significant growth within the Asia Pacific region and in order to encourage further growth particularly in the ASEAN area within the APAC region, an opportunity for a Device Registration Officer – ASIA PACIFIC OPERATION has emerged.

Info Perusahaan

Industri: Kesehatan/Medis
No. Registrasi: 9109193
Ukuran Perusahaan: 1001 - 2000 pekerja
Waktu Proses Lamaran: 23 hari
Tunjangan dan Lain-lain: Waktu regular, Senin - Jumat, Bisnis (contoh: Kemeja), will be advised during the interview
Lokasi: Cikande